K900515 is an FDA 510(k) clearance for the MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S). This device is classified as a Introducer, Catheter (Class II - Special Controls, product code DYB).
Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on August 23, 1990, 202 days after receiving the submission on February 2, 1990.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1340.
| 510(k) Number | K900515 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 02, 1990 |
| Decision Date | August 23, 1990 |
| Days to Decision | 202 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DYB — Introducer, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1340 |